A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058458



Internal ID18800989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20646773..20792462hg38UCSC Ensembl
Innerchr19:20829579..20975268hg19UCSC Ensembl
Innerchr19:20621419..20767108hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38145690
hg19145690
hg18145690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3570553, nssv3724303, nssv3570554
Samples
Known GenesZNF626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058458
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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